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Evaluation of UMELISA® T4 NEONATAL and UMELISA® T4 using polystyrene plates coated with anti-thyroxine (T4) monoclonal antibodies
Congenital hypothyroidism is one of the most common preventable causes of mental retardation. The Center of Immunoassay has developed the UMELISA® T4 NEONATAL and UMELISA® T4 to determine neonatal T4 levels in dried blood and serum samples. Both reagent kits use the same polystyrene plates coated wi...
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Published in: | Journal of immunoassay & immunochemistry 2018-01, Vol.39 (1), p.30-42 |
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creator | Castells, Elisa M. González, Ernesto C Pérez, Pedro L Del Río, Lesley Tejeda, Yileidis Perea, Yenitse Martín, Odalys Espinosa, Maryeris Rivero, Jose A. Frómeta, Amarilys |
description | Congenital hypothyroidism is one of the most common preventable causes of mental retardation. The Center of Immunoassay has developed the UMELISA® T4 NEONATAL and UMELISA® T4 to determine neonatal T4 levels in dried blood and serum samples. Both reagent kits use the same polystyrene plates coated with anti-thyroxine (T4) polyclonal antibodies as solid phase. This work shows the re-standardization of the UMELISA® T4 NEONATAL and UMELISA® T4 using plates coated with anti-T4 monoclonal antibodies (T4Mabs).
Polystyrene plates of the modified assays were firstly coated with polyclonal IgG sheep-anti-mouse IgG for 18 hours. T4Mabs were added to the plates and incubated for 2 hours at room temperature. Different performance parameters were evaluated and correlation studies with the commercial kits done.
Using polystyrene plates coated with T4Mabs increases the slope of the calibration curve in the clinical interest zone. The assay conjugates work twice diluted in respect to the ones of the commercial kits. Recovery percentages (90.8-110.7 for UMELISA® T4 NEONATAL and 92.1-109.3 for UMELISA® T4) and intra (7.2-7.6 for UMELISA® T4 NEONATAL and 6.9-7.2 for UMELISA® T4) and inter (7.4-8.5 for UMELISA® T4 NEONATAL and 7.1-8.5 for UMELISA® T4) coefficients of variation were similar to the ones described for the commercial kits. Limits of detection and quantification were 9.0 and 21.1 nmol/L for UMELISA® T4 NEONATAL, and 8.9 and 20.5 nmol/L for UMELISA® T4, respectively. The results also showed high overall concordance between assays (n = 244, r = 0.92, ρc = 0.91 for UMELISA® T4 NEONATAL and n = 492, r = 0.92, ρc = 0.9 for UMELISA® T4).
The analytical sensibility of UMELISA® T4 NEONATAL and UMELISA® T4 is improved by using polystyrene plates coated with T4Mabs, without affecting the precision and accuracy of the results.
Abbreviations: T4: L-Thyroxine; ELISA: Enzyme-linked immunosorbent assay; SUMA: Ultra Micro Analytic System; UMELISA: Ultramicro enzyme-linked immunosorbent assay; TSH: Thyroid-stimulating hormone. |
doi_str_mv | 10.1080/15321819.2017.1392321 |
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Polystyrene plates of the modified assays were firstly coated with polyclonal IgG sheep-anti-mouse IgG for 18 hours. T4Mabs were added to the plates and incubated for 2 hours at room temperature. Different performance parameters were evaluated and correlation studies with the commercial kits done.
Using polystyrene plates coated with T4Mabs increases the slope of the calibration curve in the clinical interest zone. The assay conjugates work twice diluted in respect to the ones of the commercial kits. Recovery percentages (90.8-110.7 for UMELISA® T4 NEONATAL and 92.1-109.3 for UMELISA® T4) and intra (7.2-7.6 for UMELISA® T4 NEONATAL and 6.9-7.2 for UMELISA® T4) and inter (7.4-8.5 for UMELISA® T4 NEONATAL and 7.1-8.5 for UMELISA® T4) coefficients of variation were similar to the ones described for the commercial kits. Limits of detection and quantification were 9.0 and 21.1 nmol/L for UMELISA® T4 NEONATAL, and 8.9 and 20.5 nmol/L for UMELISA® T4, respectively. The results also showed high overall concordance between assays (n = 244, r = 0.92, ρc = 0.91 for UMELISA® T4 NEONATAL and n = 492, r = 0.92, ρc = 0.9 for UMELISA® T4).
The analytical sensibility of UMELISA® T4 NEONATAL and UMELISA® T4 is improved by using polystyrene plates coated with T4Mabs, without affecting the precision and accuracy of the results.
Abbreviations: T4: L-Thyroxine; ELISA: Enzyme-linked immunosorbent assay; SUMA: Ultra Micro Analytic System; UMELISA: Ultramicro enzyme-linked immunosorbent assay; TSH: Thyroid-stimulating hormone.</description><identifier>ISSN: 1532-1819</identifier><identifier>EISSN: 1532-4230</identifier><identifier>DOI: 10.1080/15321819.2017.1392321</identifier><identifier>PMID: 29144197</identifier><language>eng</language><publisher>England: Taylor & Francis</publisher><subject>Abbreviations ; Antibodies, Monoclonal - chemistry ; Antibodies, Monoclonal - immunology ; Calibration ; Coating ; Coefficient of variation ; Congenital hypothyroidism ; Correlation analysis ; Dilution ; Enzyme-linked immunosorbent assay ; Enzyme-Linked Immunosorbent Assay - instrumentation ; Enzyme-Linked Immunosorbent Assay - methods ; Enzyme-Linked Immunosorbent Assay - standards ; Enzymes ; Humans ; Hypothyroidism ; Immunoassay ; Immunoglobulin G ; Immunoglobulins ; Mathematical analysis ; Monoclonal antibodies ; Neonates ; Plates ; Polystyrene ; Polystyrene resins ; Polystyrenes - chemistry ; Sheep ; Standardization ; SUMA technology ; Thyroid ; Thyroid gland ; Thyroid-stimulating hormone ; Thyroxine ; thyroxine (T4) ; Thyroxine - immunology ; ultra-microELISA</subject><ispartof>Journal of immunoassay & immunochemistry, 2018-01, Vol.39 (1), p.30-42</ispartof><rights>2017 Taylor & Francis 2017</rights><rights>2017 Taylor & Francis</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c309t-c0e725687598ba9bde71f45761e8d9798e8509733b5aed14c06a0fdba28aed3c3</citedby><cites>FETCH-LOGICAL-c309t-c0e725687598ba9bde71f45761e8d9798e8509733b5aed14c06a0fdba28aed3c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29144197$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Castells, Elisa M.</creatorcontrib><creatorcontrib>González, Ernesto C</creatorcontrib><creatorcontrib>Pérez, Pedro L</creatorcontrib><creatorcontrib>Del Río, Lesley</creatorcontrib><creatorcontrib>Tejeda, Yileidis</creatorcontrib><creatorcontrib>Perea, Yenitse</creatorcontrib><creatorcontrib>Martín, Odalys</creatorcontrib><creatorcontrib>Espinosa, Maryeris</creatorcontrib><creatorcontrib>Rivero, Jose A.</creatorcontrib><creatorcontrib>Frómeta, Amarilys</creatorcontrib><title>Evaluation of UMELISA® T4 NEONATAL and UMELISA® T4 using polystyrene plates coated with anti-thyroxine (T4) monoclonal antibodies</title><title>Journal of immunoassay & immunochemistry</title><addtitle>J Immunoassay Immunochem</addtitle><description>Congenital hypothyroidism is one of the most common preventable causes of mental retardation. The Center of Immunoassay has developed the UMELISA® T4 NEONATAL and UMELISA® T4 to determine neonatal T4 levels in dried blood and serum samples. Both reagent kits use the same polystyrene plates coated with anti-thyroxine (T4) polyclonal antibodies as solid phase. This work shows the re-standardization of the UMELISA® T4 NEONATAL and UMELISA® T4 using plates coated with anti-T4 monoclonal antibodies (T4Mabs).
Polystyrene plates of the modified assays were firstly coated with polyclonal IgG sheep-anti-mouse IgG for 18 hours. T4Mabs were added to the plates and incubated for 2 hours at room temperature. Different performance parameters were evaluated and correlation studies with the commercial kits done.
Using polystyrene plates coated with T4Mabs increases the slope of the calibration curve in the clinical interest zone. The assay conjugates work twice diluted in respect to the ones of the commercial kits. Recovery percentages (90.8-110.7 for UMELISA® T4 NEONATAL and 92.1-109.3 for UMELISA® T4) and intra (7.2-7.6 for UMELISA® T4 NEONATAL and 6.9-7.2 for UMELISA® T4) and inter (7.4-8.5 for UMELISA® T4 NEONATAL and 7.1-8.5 for UMELISA® T4) coefficients of variation were similar to the ones described for the commercial kits. Limits of detection and quantification were 9.0 and 21.1 nmol/L for UMELISA® T4 NEONATAL, and 8.9 and 20.5 nmol/L for UMELISA® T4, respectively. The results also showed high overall concordance between assays (n = 244, r = 0.92, ρc = 0.91 for UMELISA® T4 NEONATAL and n = 492, r = 0.92, ρc = 0.9 for UMELISA® T4).
The analytical sensibility of UMELISA® T4 NEONATAL and UMELISA® T4 is improved by using polystyrene plates coated with T4Mabs, without affecting the precision and accuracy of the results.
Abbreviations: T4: L-Thyroxine; ELISA: Enzyme-linked immunosorbent assay; SUMA: Ultra Micro Analytic System; UMELISA: Ultramicro enzyme-linked immunosorbent assay; TSH: Thyroid-stimulating hormone.</description><subject>Abbreviations</subject><subject>Antibodies, Monoclonal - chemistry</subject><subject>Antibodies, Monoclonal - immunology</subject><subject>Calibration</subject><subject>Coating</subject><subject>Coefficient of variation</subject><subject>Congenital hypothyroidism</subject><subject>Correlation analysis</subject><subject>Dilution</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Enzyme-Linked Immunosorbent Assay - instrumentation</subject><subject>Enzyme-Linked Immunosorbent Assay - methods</subject><subject>Enzyme-Linked Immunosorbent Assay - standards</subject><subject>Enzymes</subject><subject>Humans</subject><subject>Hypothyroidism</subject><subject>Immunoassay</subject><subject>Immunoglobulin G</subject><subject>Immunoglobulins</subject><subject>Mathematical analysis</subject><subject>Monoclonal antibodies</subject><subject>Neonates</subject><subject>Plates</subject><subject>Polystyrene</subject><subject>Polystyrene resins</subject><subject>Polystyrenes - chemistry</subject><subject>Sheep</subject><subject>Standardization</subject><subject>SUMA technology</subject><subject>Thyroid</subject><subject>Thyroid gland</subject><subject>Thyroid-stimulating hormone</subject><subject>Thyroxine</subject><subject>thyroxine (T4)</subject><subject>Thyroxine - immunology</subject><subject>ultra-microELISA</subject><issn>1532-1819</issn><issn>1532-4230</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp9kctuFDEQRS1ERB7wCSBLbMKiB7_64R2jaIBIk2TBZG253W7iyG0Ptjuh1_xPPoIvw52ZIJEFq6rrOrdc0gXgLUYLjBr0EZeU4AbzBUG4XmDKSdYvwNH8XjBC0ct9P0OH4DjGW4QwrxF_BQ4Jx4xlcQR-re6kHWUy3kHfw-uL1fr82_L3A9wweLm6ulxulmsoXffvZIzGfYdbb6eYpqCdhlsrk45Q-Vw6eG_STXYlU6SbKfifJhOnG_YBDt55Zb2T9nHc-s7o-Boc9NJG_WZfT8D159Xm7GuxvvpyfrZcF4oingqFdE3KqqlL3rSSt52ucc_KusK66XjNG92UiNeUtqXUHWYKVRL1XStJkzVV9ASc7vZug_8x6pjEYKLS1kqn_RgF5lVJGCdVldH3z9BbP4Z89kxxXrKMzlS5o1TwMQbdi20wgwyTwEjMKYmnlMScktinlH3v9tvHdtDdX9dTLBn4tAOM630Y5L0PthNJTtaHPkinTBT0_3_8AeueoKc</recordid><startdate>20180102</startdate><enddate>20180102</enddate><creator>Castells, Elisa M.</creator><creator>González, Ernesto C</creator><creator>Pérez, Pedro L</creator><creator>Del Río, Lesley</creator><creator>Tejeda, Yileidis</creator><creator>Perea, Yenitse</creator><creator>Martín, Odalys</creator><creator>Espinosa, Maryeris</creator><creator>Rivero, Jose A.</creator><creator>Frómeta, Amarilys</creator><general>Taylor & Francis</general><general>Marcel Dekker, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20180102</creationdate><title>Evaluation of UMELISA® T4 NEONATAL and UMELISA® T4 using polystyrene plates coated with anti-thyroxine (T4) monoclonal antibodies</title><author>Castells, Elisa M. ; González, Ernesto C ; Pérez, Pedro L ; Del Río, Lesley ; Tejeda, Yileidis ; Perea, Yenitse ; Martín, Odalys ; Espinosa, Maryeris ; Rivero, Jose A. ; Frómeta, Amarilys</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c309t-c0e725687598ba9bde71f45761e8d9798e8509733b5aed14c06a0fdba28aed3c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Abbreviations</topic><topic>Antibodies, Monoclonal - chemistry</topic><topic>Antibodies, Monoclonal - immunology</topic><topic>Calibration</topic><topic>Coating</topic><topic>Coefficient of variation</topic><topic>Congenital hypothyroidism</topic><topic>Correlation analysis</topic><topic>Dilution</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Enzyme-Linked Immunosorbent Assay - instrumentation</topic><topic>Enzyme-Linked Immunosorbent Assay - methods</topic><topic>Enzyme-Linked Immunosorbent Assay - standards</topic><topic>Enzymes</topic><topic>Humans</topic><topic>Hypothyroidism</topic><topic>Immunoassay</topic><topic>Immunoglobulin G</topic><topic>Immunoglobulins</topic><topic>Mathematical analysis</topic><topic>Monoclonal antibodies</topic><topic>Neonates</topic><topic>Plates</topic><topic>Polystyrene</topic><topic>Polystyrene resins</topic><topic>Polystyrenes - chemistry</topic><topic>Sheep</topic><topic>Standardization</topic><topic>SUMA technology</topic><topic>Thyroid</topic><topic>Thyroid gland</topic><topic>Thyroid-stimulating hormone</topic><topic>Thyroxine</topic><topic>thyroxine (T4)</topic><topic>Thyroxine - immunology</topic><topic>ultra-microELISA</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Castells, Elisa M.</creatorcontrib><creatorcontrib>González, Ernesto C</creatorcontrib><creatorcontrib>Pérez, Pedro L</creatorcontrib><creatorcontrib>Del Río, Lesley</creatorcontrib><creatorcontrib>Tejeda, Yileidis</creatorcontrib><creatorcontrib>Perea, Yenitse</creatorcontrib><creatorcontrib>Martín, Odalys</creatorcontrib><creatorcontrib>Espinosa, Maryeris</creatorcontrib><creatorcontrib>Rivero, Jose A.</creatorcontrib><creatorcontrib>Frómeta, Amarilys</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of immunoassay & immunochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Castells, Elisa M.</au><au>González, Ernesto C</au><au>Pérez, Pedro L</au><au>Del Río, Lesley</au><au>Tejeda, Yileidis</au><au>Perea, Yenitse</au><au>Martín, Odalys</au><au>Espinosa, Maryeris</au><au>Rivero, Jose A.</au><au>Frómeta, Amarilys</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of UMELISA® T4 NEONATAL and UMELISA® T4 using polystyrene plates coated with anti-thyroxine (T4) monoclonal antibodies</atitle><jtitle>Journal of immunoassay & immunochemistry</jtitle><addtitle>J Immunoassay Immunochem</addtitle><date>2018-01-02</date><risdate>2018</risdate><volume>39</volume><issue>1</issue><spage>30</spage><epage>42</epage><pages>30-42</pages><issn>1532-1819</issn><eissn>1532-4230</eissn><abstract>Congenital hypothyroidism is one of the most common preventable causes of mental retardation. The Center of Immunoassay has developed the UMELISA® T4 NEONATAL and UMELISA® T4 to determine neonatal T4 levels in dried blood and serum samples. Both reagent kits use the same polystyrene plates coated with anti-thyroxine (T4) polyclonal antibodies as solid phase. This work shows the re-standardization of the UMELISA® T4 NEONATAL and UMELISA® T4 using plates coated with anti-T4 monoclonal antibodies (T4Mabs).
Polystyrene plates of the modified assays were firstly coated with polyclonal IgG sheep-anti-mouse IgG for 18 hours. T4Mabs were added to the plates and incubated for 2 hours at room temperature. Different performance parameters were evaluated and correlation studies with the commercial kits done.
Using polystyrene plates coated with T4Mabs increases the slope of the calibration curve in the clinical interest zone. The assay conjugates work twice diluted in respect to the ones of the commercial kits. Recovery percentages (90.8-110.7 for UMELISA® T4 NEONATAL and 92.1-109.3 for UMELISA® T4) and intra (7.2-7.6 for UMELISA® T4 NEONATAL and 6.9-7.2 for UMELISA® T4) and inter (7.4-8.5 for UMELISA® T4 NEONATAL and 7.1-8.5 for UMELISA® T4) coefficients of variation were similar to the ones described for the commercial kits. Limits of detection and quantification were 9.0 and 21.1 nmol/L for UMELISA® T4 NEONATAL, and 8.9 and 20.5 nmol/L for UMELISA® T4, respectively. The results also showed high overall concordance between assays (n = 244, r = 0.92, ρc = 0.91 for UMELISA® T4 NEONATAL and n = 492, r = 0.92, ρc = 0.9 for UMELISA® T4).
The analytical sensibility of UMELISA® T4 NEONATAL and UMELISA® T4 is improved by using polystyrene plates coated with T4Mabs, without affecting the precision and accuracy of the results.
Abbreviations: T4: L-Thyroxine; ELISA: Enzyme-linked immunosorbent assay; SUMA: Ultra Micro Analytic System; UMELISA: Ultramicro enzyme-linked immunosorbent assay; TSH: Thyroid-stimulating hormone.</abstract><cop>England</cop><pub>Taylor & Francis</pub><pmid>29144197</pmid><doi>10.1080/15321819.2017.1392321</doi><tpages>13</tpages></addata></record> |
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source | Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Science and Technology Collection (Reading list) |
subjects | Abbreviations Antibodies, Monoclonal - chemistry Antibodies, Monoclonal - immunology Calibration Coating Coefficient of variation Congenital hypothyroidism Correlation analysis Dilution Enzyme-linked immunosorbent assay Enzyme-Linked Immunosorbent Assay - instrumentation Enzyme-Linked Immunosorbent Assay - methods Enzyme-Linked Immunosorbent Assay - standards Enzymes Humans Hypothyroidism Immunoassay Immunoglobulin G Immunoglobulins Mathematical analysis Monoclonal antibodies Neonates Plates Polystyrene Polystyrene resins Polystyrenes - chemistry Sheep Standardization SUMA technology Thyroid Thyroid gland Thyroid-stimulating hormone Thyroxine thyroxine (T4) Thyroxine - immunology ultra-microELISA |
title | Evaluation of UMELISA® T4 NEONATAL and UMELISA® T4 using polystyrene plates coated with anti-thyroxine (T4) monoclonal antibodies |
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